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Learn MoreProtect Trial Participants We’ve been patient-centric since the beginning, and our research review services are unmatched in the category. Learn MoreDeliver Innovation We don’t rest in our mission to make clinical research safer, smarter, and faster for patients, sites, sponsors and CROs. Learn MoreProven Clinical Research Services and Technology #1 in Trusted Research Review Services Learn More#1 in Connected Site and Sponsor Technology Learn MoreReimagining the Clinical Research Experience Learn MoreTop Clinical Research Sponsors, CROs, and Sites Partner with Advarra to Accelerate Their Clinical Research 3,500+ institutions, hospitals, health systems, and academic medical centers trust Advarra. 50K investigators utilize Advarra trial technology solutions to support their research. 12K+ open protocols overseen by Advarra annually 78% of NCI-designated Cancer Centers use Advarra technology. Bring Your Clinical Trial Together Advarra’s IRB and IBC reviews and Gene Therapy Ready site network helped reduce study startup timelines and delivered trial results to IQVIA quicker than expected. Case StudyAt Inova Health System, the research team improved regulatory efficiency by 20% without the need for extra regulatory staff by adopting Advarra’s eRegulatory Management System. Case StudyUsing Advarra Insights, The University of Wisconsin Carbone Cancer Center was able to enhance their data analytics and visualization capabilities. Case StudyAdvarra served as the institutional review board (IRB) of record for the phase I trial for the first-in-human dose-escalation study of an mRNA Vaccine Against SARS-CoV-2. Learn MoreLongboat: The Reimagined Clinical Trial Experience Longboat is the single hub to centralize, connect, and simplify your clinical trials Create a central hub for a study to reduce burden and increase visibility Modern, simple technology that sites want to use Faster startup and improved regulatory process efficiency Learn More The 2023 Study Activation Report Hear from clinical researchers striving to get life-saving therapies into the market. Read about How a proliferation of technology and process is creating delays and adding administrative burdens that stall clinical research progress. What sponsors and CROs are doing to reduce site feasibility burdens. Which technology improvements are impacting study activation strategies. Read the Report Are You Ready to Bring People Together for Better, Faster Trial Outcomes? Learn More Scroll to Top Subscribe to our monthly email Receive updates monthly about webinars for CEUs, white papers, podcasts, and more. 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